Canonical Allele Identifier: PA2827616365
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 448313
ClinVar RCV Id: RCV000517993 RCV000551603 RCV002448560
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.His799Tyr
CA5297604
NM_001351527.2:c.2395C>T